Formononetin

• Catalog No.: 47752
• CAS Number: 485-72-3
• M. F.: C16H12O4
• M. W.: 268.26408
• Purity: ≥99.0% (TLC)

SYNONYMS

• IUPAC name: 7-hydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one
• IUPAC Traditional name: formononetin
• Synonyms: 7-Hydroxy-3-(4-methoxyphenyl)chromone; 7-Hydroxy-4′-methoxyisoflavone

DATABASE IDS

• MDL Number: MFCD00016948
• EC Number: 207-623-9
• Beilstein Number: 237979
• PubChem SID: 24871382
• CAS Number: 485-72-3

PROPERTIES

• Empirical Formula (Hill Notation): C16H12O4
• Purity: ≥99.0% (TLC)
• Melting Point: 257-261 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Biochem/physiol Actions
Isoflavone found in red clover. Effective against Giardia lamblia infection, at least partially by inducing detachment of trophozoites from intestinal mucosa.1
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 47752.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Description (简体中文)

Biochem/physiol Actions
Isoflavone found in red clover. Effective against Giardia lamblia infection, at least partially by inducing detachment of trophozoites from intestinal mucosa.1
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 47752.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.